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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776309Generated: October 31, 2026

N-bromobutanimide → 4-bromo-2,2-dimethyl-5-(pyridin-4-yl)furan-3(2H)-one

https://huagongshe.com/reaction/1776309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2,2-dimethyl-5-(pyridin-4-yl)furan-3(2H)-oneHCID 59354790—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
Product4-bromo-2,2-dimethyl-5-(pyridin-4-yl)furan-3(2H)-oneHCID 5935482422%

Reaction Steps

To a room temperature, stirred solution of 2,2-dimethyl-5-(pyridin-4-yl)furan-3(2H)-one (0.81 g, 4.28 mmol) in CHCl3 (20 mL), NBS (1.3 g, 7.28 mmol) was added portionwise. The reaction mixture was then stirred for 2 h and diluted with DCM (100 mL). The combined organic layers were washed with water (50 mL) and brine (50 mL), dried over Na2SO4, filtered, and then concentrated in vacuo to obtain the crude product. The crude material was purified via silica gel column chromatography to afford 4-bromo-2,2-dimethyl-5-(pyridin-4-yl)furan-3(2H)-one (0.25 g, 22%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09265767B2
Source datasetuspto-grants-2016_02
ORD IDord-ca6d2561063b49779127fb0555367277
Source noteuspto-grants-2016_02